rs1064797197
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
15
Location
31026162
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3606G>T (p.Glu1202Asp)
Allele
A
Clinical Significance
Uncertain significance